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Page 1
Social deprivation is associated with poor kidney transplantation outcome in children.
Driollet B, Bayer F, Chatelet V, Macher MA, Salomon R, Ranchin B, Roussey G, Lahoche A, Garaix F, Decramer S, Mérieau E, Fila M, Zaloszyc A, Deschênes G, Valeri L, Launay L, Couchoud C, Leffondré K, Harambat J. Driollet B, et al. Among authors: macher ma. Kidney Int. 2019 Sep;96(3):769-776. doi: 10.1016/j.kint.2019.05.011. Epub 2019 May 28. Kidney Int. 2019. PMID: 31375259 Free article.
Prognosis of lupus membranous nephropathy in children.
Nathanson S, Salomon R, Ranchin B, Macher MA, Lavocat MP, Krier MJ, Baudouin V, Azéma C, Bader-Meunier B, Deschênes G. Nathanson S, et al. Among authors: macher ma. Pediatr Nephrol. 2006 Aug;21(8):1113-6. doi: 10.1007/s00467-006-0129-z. Epub 2006 Jun 30. Pediatr Nephrol. 2006. PMID: 16810516
Darbepoetin, effective treatment of anaemia in paediatric patients with chronic renal failure.
André JL, Deschênes G, Boudailliez B, Broux F, Fischbach M, Gagnadoux MF, Horen B, Lahoche-Manucci A, Macher MA, Roussel B, Tsimaratos M, Loirat C. André JL, et al. Among authors: macher ma. Pediatr Nephrol. 2007 May;22(5):708-14. doi: 10.1007/s00467-006-0402-1. Epub 2007 Jan 11. Pediatr Nephrol. 2007. PMID: 17216497 Free PMC article. Clinical Trial.
Differential impact of complement mutations on clinical characteristics in atypical hemolytic uremic syndrome.
Sellier-Leclerc AL, Fremeaux-Bacchi V, Dragon-Durey MA, Macher MA, Niaudet P, Guest G, Boudailliez B, Bouissou F, Deschenes G, Gie S, Tsimaratos M, Fischbach M, Morin D, Nivet H, Alberti C, Loirat C; French Society of Pediatric Nephrology. Sellier-Leclerc AL, et al. Among authors: macher ma. J Am Soc Nephrol. 2007 Aug;18(8):2392-400. doi: 10.1681/ASN.2006080811. Epub 2007 Jun 28. J Am Soc Nephrol. 2007. PMID: 17599974
Phenotype-genotype correlation in antenatal and neonatal variants of Bartter syndrome.
Brochard K, Boyer O, Blanchard A, Loirat C, Niaudet P, Macher MA, Deschenes G, Bensman A, Decramer S, Cochat P, Morin D, Broux F, Caillez M, Guyot C, Novo R, Jeunemaître X, Vargas-Poussou R. Brochard K, et al. Among authors: macher ma. Nephrol Dial Transplant. 2009 May;24(5):1455-64. doi: 10.1093/ndt/gfn689. Epub 2008 Dec 18. Nephrol Dial Transplant. 2009. PMID: 19096086
Effect of conservative treatment on the renal outcome of children with primary hyperoxaluria type 1.
Fargue S, Harambat J, Gagnadoux MF, Tsimaratos M, Janssen F, Llanas B, Berthélémé JP, Boudailliez B, Champion G, Guyot C, Macher MA, Nivet H, Ranchin B, Salomon R, Taque S, Rolland MO, Cochat P. Fargue S, et al. Among authors: macher ma. Kidney Int. 2009 Oct;76(7):767-73. doi: 10.1038/ki.2009.237. Epub 2009 Jul 1. Kidney Int. 2009. PMID: 19571789 Free article.
Genotype-phenotype correlation in primary hyperoxaluria type 1: the p.Gly170Arg AGXT mutation is associated with a better outcome.
Harambat J, Fargue S, Acquaviva C, Gagnadoux MF, Janssen F, Liutkus A, Mourani C, Macher MA, Abramowicz D, Legendre C, Durrbach A, Tsimaratos M, Nivet H, Girardin E, Schott AM, Rolland MO, Cochat P. Harambat J, et al. Among authors: macher ma. Kidney Int. 2010 Mar;77(5):443-9. doi: 10.1038/ki.2009.435. Epub 2009 Dec 16. Kidney Int. 2010. PMID: 20016466 Free article.
Rituximab efficiency in children with steroid-dependent nephrotic syndrome.
Sellier-Leclerc AL, Macher MA, Loirat C, Guérin V, Watier H, Peuchmaur M, Baudouin V, Deschênes G. Sellier-Leclerc AL, et al. Among authors: macher ma. Pediatr Nephrol. 2010 Jun;25(6):1109-15. doi: 10.1007/s00467-010-1465-6. Epub 2010 Mar 18. Pediatr Nephrol. 2010. PMID: 20238230 Clinical Trial.
97 results